Canonical Allele Identifier: PA2829391816
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 409849

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002867.1:p.Phe6Tyr
CA8677122
NM_002876.4:c.17T>A